Cancer data collection begins by identifying people with cancer who have been diagnosed or received cancer care in hospitals, outpatient clinics, radiology departments, doctors' offices, laboratories, surgical centers, or from other providers (such as pharmacists) who diagnose or treat cancer patients..
Is there a database for cancer patients?
The NCDB is a clinical oncology database sourced from hospital registry data collected in more than 1,500 Commission on Cancer-accredited facilities. These data are used to analyze and track patients with malignant neoplastic diseases, their treatments, and outcomes..
Which data is important to collect in a patient with cancer?
A complete and detailed collection of data about every cancer is the key to understanding this complex disease – the symptoms people have, how their cancer is diagnosed, how they respond to treatment and how their own cancer progresses over time.Feb 4, 2016.
Which data is important to collect in a patient with cancer?
Treatment: Treatment information captures the various options selected to treat the cancer patient, such as surgery, radiation therapy, chemotherapy, hormone therapy, and immunotherapy. Outcomes:Outcomes information consists of patient's vital status, cause of death, and survival time..
Why is it necessary to collect and report on cancer patients data?
A complete and detailed collection of data about every cancer is the key to understanding this complex disease – the symptoms people have, how their cancer is diagnosed, how they respond to treatment and how their own cancer progresses over time.Feb 4, 2016.
Why is it necessary to collect and report on data about cancer patients?
Population-based registries are designed to: determine cancer patterns among various populations or sub-populations. monitor cancer trends over time. guide planning and evaluation of cancer control efforts..
Behind the system are people, cancer registrars, who are responsible for collecting the cancer data and making sure they are timely, accurate, and complete.
Clinical cancer researchers conduct clinical trials, study a particular patient or group of patients, including their behaviors, or use materials from humans, such as blood or tissue samples, to learn about disease, how the healthy body works, or how it responds to treatment.
At the hospital's cancer registry, a specially trained person called a cancer registrar enters information about the cancer and treatment from Jennifer's medical record into a computer. The hospital registry sends this information to the central cancer registry in its state.
Cancer data collection begins by identifying people with cancer who have been diagnosed or received medical care in hospitals, outpatient clinics, radiology departments, doctors' offices, laboratories, surgical centers, or from other providers who diagnose or treat cancer patients.
The information collected by cancer registries can be placed into several categories: Patient demographics: Patient demographic information identifies the cancer patient. It includes the patient's name, age, gender, race, ethnicity, and birthplace.
How many cancer datasets are there?
There are 41 cancer datasets available on data
world
Find open data about cancer contributed by thousands of users and organizations across the world
The rates are the numbers out of 100,000 people who developed or died from cancer each year
Number of Cancer Surgeries (Volume) Performed in Californ
What is a cancer statistics data visualization tool?
The U S
Cancer Statistics Data Visualizations tool provides information on the numbers and rates of new cancer cases and deaths at the national, state, and county levels
You can see the numbers by sex, age, race and ethnicity, trends over time, survival, and prevalence
Text explains what is shown on each chart and graph
What is cancer data collection?
Cancer data collection begins by identifying people with cancer who have been diagnosed or received cancer care in hospitals, outpatient clinics, radiology departments, doctors’ offices, laboratories, surgical centers, or from other providers (such as pharmacists) who diagnose or treat cancer patients
Cancer registry data collection involves, at a minimum, collecting data on demographics, tumor characteristics, and treatment. A common, identified, and standardized set of data elements is needed to share data quickly and efficiently with consumers of this data.
Data collection cancer patients
U.S. research cooperative group
Cancer and Leukemia Group B is a cancer research cooperative group in the United States.
A cancer registry is a systematic collection of data about cancer and tumor diseases. The data are collected by Cancer Registrars. Cancer Registrars capture a complete summary of patient history, diagnosis, treatment, and status for every cancer patient in the United States, and other countries.
An electronic patient-reported outcome (ePRO) is a patient-reported outcome that is collected by electronic methods. ePRO methods are most commonly used in clinical trials, but they are also used elsewhere in health care. As a function of the regulatory process, a majority of ePRO questionnaires undergo the linguistic validation process. When the data is captured for a clinical trial, the data is considered a form of Electronic Source Data.
Database of medical images for cancer research
The Cancer Imaging Archive (TCIA) is an open-access database of medical images for cancer research. The site is funded by the National Cancer Institute's (NCI) Cancer Imaging Program, and the contract is operated by the University of Arkansas for Medical Sciences. Data within the archive is organized into collections which typically share a common cancer type and/or anatomical site. The majority of the data consists of CT, MRI, and nuclear medicine images stored in DICOM format, but many other types of supporting data are also provided or linked to, in order to enhance research utility. All data are de-identified in order to comply with the Health Insurance Portability and Accountability Act and National Institutes of Health data sharing policies.
